rs138687036
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;T) | 3 | Carrier of G6PD deficiency mutation; variable expressivity |
(T;T) | 5 | G6PD deficiency |
is a | snp |
is | mentioned by |
dbSNP | rs138687036 |
dbSNP (classic) | rs138687036 |
ClinGen | rs138687036 |
ebi | rs138687036 |
HLI | rs138687036 |
Exac | rs138687036 |
Gnomad | rs138687036 |
Varsome | rs138687036 |
LitVar | rs138687036 |
Map | rs138687036 |
PheGenI | rs138687036 |
Biobank | rs138687036 |
1000 genomes | rs138687036 |
hgdp | rs138687036 |
ensembl | rs138687036 |
geneview | rs138687036 |
scholar | rs138687036 |
rs138687036 | |
pharmgkb | rs138687036 |
gwascentral | rs138687036 |
openSNP | rs138687036 |
23andMe | rs138687036 |
SNPshot | rs138687036 |
SNPdbe | rs138687036 |
MSV3d | rs138687036 |
GWAS Ctlg | rs138687036 |
Max Magnitude | 5 |
aka c.241C>T (p.Arg81Cys)